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Hemolysis clinical trials

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NCT ID: NCT02464891 Terminated - Clinical trials for Atypical Hemolytic Uremic Syndrome

Complement Inhibition in aHUS Dialysis Patients

ACCESS
Start date: June 4, 2015
Phase: Phase 2
Study type: Interventional

This study evaluates the effect of CCX168, a C5aR Antagonist, Oral Administration on Ex Vivo Thrombus Formation and Disease Activity in ten patients with diagnosis of Atypical Hemolytic Uremic Syndrome with or without genetic abnormalities in the complement system or thrombomodulin, on stable chronic extracorporeal or peritoneal dialysis therapy since at least 6 months.

NCT ID: NCT01522170 Terminated - Clinical trials for Atypical Hemolytic Uremic Syndrome

aHUS Observational Long Term Follow-Up

LTFU
Start date: March 2012
Phase: N/A
Study type: Observational [Patient Registry]

There is growing but limited information on the long term clinical status of aHUS patients who have previously received or are continuing to receive treatment with eculizumab. This study is designed to collect clinical data that will provide insight into the long-term outcomes of patients with aHUS.

NCT ID: NCT00102245 Terminated - Hemoglobinopathies Clinical Trials

Clinical and Laboratory Investigation of Humans With Informative Iron or Erythroid Phenotypes

Start date: January 18, 2005
Phase: N/A
Study type: Observational

This study will examine blood for factors that may cause or prevent diseases involving iron or red blood cells. Iron is an important nutrient for human health that is needed to produce red blood cells. Red blood cells carry oxygen to body tissues. A better understanding of iron and red blood cells may help lead to better treatment of several diseases including anemia. Patients of all ages with red cell abnormalities in the following categories may be eligible for this study: - Diseases with deficiency, overload or maldistribution of iron - Known red blood cell diseases, such as anemias and hemoglobinopathies - Red blood cell diseases of unknown cause, such as hemolysis of unknown cause - Red blood cell abnormalities with no overt clinical disease, such as hereditary persistence of fetal hemoglobin Participants undergo the following procedures: - Medical history - Physical examination - Standard medical tests related to the individual's iron or red blood cell condition Blood draw for the following purposes: - Testing for syphilis and for the hepatitis B and C, HIV, and HTLV-1viruses, and for a pregnancy test for women who can become pregnant - Research purposes. This blood is analyzed for genes, proteins, sugars, and fat molecules.

NCT ID: NCT00004465 Terminated - Clinical trials for Hemolytic Uremic Syndrome

Phase III Randomized Study of SYNSORB Pk in Children With E. Coli-Associated Hemolytic Uremic Syndrome

Start date: July 27, 1997
Phase: Phase 3
Study type: Interventional

OBJECTIVES: I. Determine the effect of SYNSORB Pk therapy on mortality and frequency of severe extrarenal complications observed in children with acute stage E. coli-associated hemolytic uremic syndrome. II. Determine the effect of SYNSORB Pk therapy on the need for the duration of dialysis in these patients. III. Determine the effect of SYNSORB Pk therapy on the recovery of renal function and resolution of urinary abnormalities in these patients.